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The Chemistry of Powder and Explosives - Sciencemadness Dot Org

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BUTYL TETRYL 183<br />

MINIMUM CHARGE FOB DETONATION OF<br />

TNT Tetryl<br />

Mercuric fulminate 0.36 0.29<br />

Silver fulminate 0.095 0.02<br />

Cadmium fulminate 0.11 0.008<br />

Mercurous azide 0.145 0.045<br />

Silver azide 0.07 0.02<br />

Lead azide 0.09 0.025<br />

Cadmium azide 0.04 0.01<br />

With each <strong>of</strong> the initiators which was tried, tetryl was more easily<br />

detonated than TNT. Taylor <strong>and</strong> Cope 100 have determined the<br />

minimum charges <strong>of</strong> fulminate-chlorate (90:10) necessary to<br />

cause the complete detonation <strong>of</strong> various mixtures <strong>of</strong> TNT <strong>and</strong><br />

tetryl, as follows:<br />

MIXTURE OF TNT-TETRYL WEIGHT OF INITIATOR, GRAMS<br />

100 0 0.25<br />

90 10 0.22<br />

80 20 0.21<br />

50 50 0.20<br />

0 100 0.19<br />

"Ethyl Tetryl." 2,4,6-Trinitrophenylethylnitramine<br />

<strong>The</strong> ethyl analogue <strong>of</strong> tetryl was first prepared by van Romburgh,<br />

101 who procured it both by nitrating monoethylaniline <strong>and</strong><br />

by nitrating diethylaniline, <strong>and</strong> reported that it melts at 96°.<br />

<strong>The</strong> present writer has found that the pure material, recrystallized<br />

twice from nitric acid (d. 1.42) <strong>and</strong> once from alcohol,<br />

melts at 94°. It is comparable to tetryl in its chemical reactions<br />

<strong>and</strong> in its explosive properties.<br />

"Butyl Tetryl." 2,4,6-Trinitrophenyl-w-butylnitramine<br />

<strong>The</strong> w-butyl analogue <strong>of</strong> tetryl 102 has been prepared by two<br />

methods: (a) by condensing 2,4-dinitrochlorobenzene with<br />

n-butylamine to form 2,4-dinitro-n-butylaniline, 103 <strong>and</strong> by the<br />

nitration <strong>of</strong> this product; <strong>and</strong> (b) by the nitration in one step <strong>of</strong><br />

n-butylaniline. <strong>The</strong> pure substance crystallizes from alcohol in<br />

100 U. S. Bureuu cj Mines Technical Paper 145, Washington, 1916.<br />

101 Rec. Irav. chim., 2, 111 (1883).<br />

103 Davis, U. S. Pat. 1,607,059 (1926).<br />

103 pure 2,4-dinitro-n-butylaniline crystallizes from alcohol in deep yellow<br />

or orange needles, m.p. 92.5-93.0°.

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